Publications

Sun L, Surya S, Goodman NG, Le AN, Kelly G, Owoyemi O, Desai H, Zheng C, DeLuca S, Good ML, Hussain J, Jeffries SD, Kry YR, Kugler EM, Mansour M, Ndicu J, Osei-Akoto A, Prior T, Pundock SL, Varughese LA, Weaver J, Doucette A, Dudek S, Verma SS, Gouma S, Weirick ME, McAllister CM, Bange E, Gabriel P, Ritchie M, Rader DJ, Vonderheide RH, Schuchter LM, Verma A, Maillard I, Mamtani R, Hensley SE, Gross R, Wileyto EP, Huang AC, Maxwell KN, DeMichele A.  SARS-CoV-2 seropositivity and seroconversion in patients undergoing active cancer-directed therapy.  medRxiv. 2021 Jan 16:2021.01.15.21249810. doi: 10.1101/2021.01.15.21249810. Preprint.PMID: 33469597

 

Liu X, Verma A, Ramage H, Garcia G, Myers RL, Lucas A, Michaelson JJ, Coryell W, Kumar A, Charney A, Kazanietz MG, Rader DJ, Ritchie MD, Berrettini WH, Damoiseaux R, Arumugaswami V, Schultz D, Cherry S, Klein PS. Targeting the Coronavirus Nucleocapsid Protein through GSK-3 Inhibition. medRxiv. 2021 Feb 22:2021.02.17.21251933. doi: 10.1101/2021.02.17.21251933. Preprint. PMID: 33655282 Free PMC article.

 

Kosmicki JA, Horowitz JE, Banerjee N, Lanche R, Marcketta A, Maxwell E, Bai X, Sun D, Backman JD, Sharma D, Kang HM, O'Dushlaine C, Yadav A, Mansfield AJ, Li AH, Watanabe K, Gurski L, McCarthy SE, Locke AE, Khalid S, O'Keeffe S, Mbatchou J, Chazara O, Huang Y, Kvikstad E, O'Neill A, Nioi P, Parker MM, Petrovski S, Runz H, Szustakowski JD, Wang Q, Wong E, Cordova-Palomera A, Smith EN, Szalma S, Zheng X, Esmaeeli S, Davis JW, Lai YP, Chen X, Justice AE, Leader JB, Mirshahi T, Carey DJ, Verma A, Sirugo G, Ritchie MD, Rader DJ, Povysil G, Goldstein DB, Kiryluk K, Pairo-Castineira E, Rawlik K, Pasko D, Walker S, Meynert A, Kousathanas A, Moutsianas L, Tenesa A, Caulfield M, Scott R, Wilson JF, Baillie JK, Butler-Laporte G, Nakanishi T, Lathrop M, Richards JB, Jones M, Balasubramanian S, Salerno W, Shuldiner AR, Marchini J, Overton JD, Habegger L, Cantor MN, Reid JG, Baras A, Abecasis GR, Ferreira MA. A catalog of associations between rare coding variants and COVID-19 outcomes. medRxiv. 2021 Feb 27:2020. 10.28.20221804. doi: 10.1101/2020.10.28.20221804. Preprint. PMID: 33655273 Free PMC article.

 

Sun L, Surya S, Le AN, Desai H, Doucette A, Gabriel P, Ritchie MD, Rader D, Maillard I, Bange E, Huang AC, Vonderheide RH, DeMichele A, Verma A, Mamtani R, Maxwell KN. Rates of COVID-19-Related Outcomes in Cancer Compared With Noncancer Patients. JNCI Cancer Spectr. 2021 Jan 21;5(1):pkaa120. doi: 10.1093/jncics/pkaa120. eCollection 2021 Feb.PMID: 33554040 Free PMC article.

 

Horowitz JE, Kosmicki JA, Damask A, Sharma D, Roberts GHL, Justice AE, Banerjee N, Coignet MV, Yadav A, Leader JB, Marcketta A, Park DS, Lanche R, Maxwell E, Knight SC, Bai X, Guturu H, Sun D, Baltzell A, Kury FSP, Backman JD, Girshick AR, O'Dushlaine C, McCurdy SR, Partha R, Mansfield AJ, Turissini DA, Li AH, Zhang M, Mbatchou J, Watanabe K, Gurski L, McCarthy SE, Kang HM, Dobbyn L, Stahl E, Verma A, Sirugo G, Ritchie MD, Jones M, Balasubramanian S, Siminovitch K, Salerno WJ, Shuldiner AR, Rader DJ, Mirshahi T, Locke AE, Marchini J, Overton JD, Carey DJ, Habegger L, Cantor MN, Rand KA, Hong EL, Reid JG, Ball CA, Baras A, Abecasis GR, Ferreira MA. Common genetic variants identify targets for COVID-19 and individuals at high risk of severe disease. medRxiv. 2021 Feb 19:2020.12.14.20248176. doi: 10.1101/2020.12.14.20248176. Preprint. PMID: 33619501 Free PMC article.

 

Gu, X., Yang, H., Sheng, X., Ko, Y. A., Qiu, C., Park, J., Huang, S., Kember, R., Judy, R. L., Park, J., Damrauer, S. M., Nadkarni, G., Loos, R. J. F., My, V. T. H., Chaudhary, K., Bottinger, E. P., Paranjpe, I., Saha, A., Brown, C., Akilesh, S., Hung, A. M., Palmer, M., Baras, A., Overton, J. D., Reid, J., Ritchie, M., Rader, D. J. & Susztak, K. Kidney disease genetic risk variants alter lysosomal beta-mannosidase (MANBA) expression and disease severity. Sci. Transl. Med. 13, (2021).

 

Park, J., Lucas, A. M., Zhang, X., Chaudhary, K., Cho, J. H., Nadkarni, G., Dobbyn, A., Chittoor, G., Josyula, N. S., Katz, N., Breeyear, J. H., Ahmadmehrabi, S., Drivas, T. G., Chavali, V. R. M., Fasolino, M., Sawada, H., Daugherty, A., Li, Y., Zhang, C., Bradford, Y., Weaver, J. E., Verma, A., Judy, R. L., Kember, R. L., Overton, J. D., Reid, J. G., Ferreira, M. A. R., Li, A. H., Baras, A., LeMaire, S. A., Shen, Y. H., Naji, A., Kaestner, K. H., Vahedi, G., Edwards, T. L., Chen, J., Damrauer, S. M., Justice, A. E., Do, R., Ritchie, M. D. & Rader, D. J. Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations. Nat. Med. 27, 66–72 (2021).

 

Lau-Min KS, Asher SB, Chen J, Domchek SM, Feldman M, Joffe S, Landgraf J, Speare V, Varughese LA, Tuteja S, VanZandbergen C, Ritchie MD, Nathanson KL. Real-world integration of genomic data into the electronic health record: the PennChart Genomics Initiative. Genet Med. 2020 Dec 10. doi: 10.1038/s41436-020-01056-y. Online ahead of print. PMID: 33299147 No abstract available.

 

Vasta, L. M., McMaster, M. L., Harney, L. A., Ling, A., Kim, J., Harris, A. K., Carr, A. G., Damrauer, S. M., Rader, D. J., Kember, R. L., Kanetsky, P. A., Nathanson, K. L., Pyle, L. C., Greene, M. H., Schultz, K. A., Stewart, D. R. & Regeneron Genetics Center (RGC) Research Team. Lack of pathogenic germline DICER1 variants in males with testicular germ-cell tumors. Cancer Genet. 248–249, 49–56 (2020).

 

Anderson EM, Goodwin EC, Verma A, Arevalo CP, Bolton MJ, Weirick ME, Gouma S, McAllister CM, Christensen SR, Weaver J, Hicks P, Manzoni TB, Oniyide O, Ramage H, Mathew D, Baxter AE, Oldridge DA, Greenplate AR, Wu JE, Alanio C, D'Andrea K, Kuthuru O, Dougherty J, Pattekar A, Kim J, Han N, Apostolidis SA, Huang AC, Vella LA, Kuri-Cervantes L, Pampena MB; UPenn COVID Processing Unit, Betts MR, Wherry EJ, Meyer NJ, Cherry S, Bates P, Rader DJ, Hensley SE.   Seasonal human coronavirus antibodies are boosted upon SARS-CoV-2 infection but not associated with protection.   Cell. 2021 Feb 9:S0092-8674(21)00160-4. doi: 10.1016/j.cell.2021.02.010. Online ahead of print.PMID: 33631096 

 

Flannery DD, Gouma S, Dhudasia MB, Mukhopadhyay S, Pfeifer MR, Woodford EC, Gerber JS, Arevalo CP, Bolton MJ, Weirick ME, Goodwin EC, Anderson EM, Greenplate AR, Kim J, Han N, Pattekar A, Dougherty J, Kuthuru O, Mathew D, Baxter AE, Vella LA, Weaver J, Verma A, Leite R, Morris JS, Rader DJ, Elovitz MA, Wherry EJ, Puopolo KM, Hensley SE.   SARS-CoV-2 seroprevalence among parturient women in Philadelphia. Sci Immunol. 2020 Jul 29;5(49):eabd5709. doi: 10.1126/sciimmunol.abd5709.PMID: 32727884 

 

Kember RL, Merikangas AK, Verma SS, Verma A, Judy R; Regeneron Genetics Center, Damrauer SM, Ritchie MD, Rader DJ, Bućan M. Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals. Biol Psychiatry. 2021 Feb 1;89(3):236-245. doi: 10.1016/j.biopsych.2020.06.026. Epub 2020 Jul 6. PMID: 32919613

 

Verma SS, Chung WK, Dudek S, Williamson JL, Verma A, Robinson S, Rader DJ, Reilly MP, Sengupta S, FitzGerald GA, Kiryluk K, and Ritchie MD. Research on COVID-19 through patient-reported data: a survey for observational studies in the COVID-19 pandemic. Journal of Clinical and Translational Science. First View, pp. 1 – 5: https://doi.org/10.1017/cts.2020.509

 

Levin, M. G., Judy, R., Gill, D., Vujkovic, M., Verma, S. S., Bradford, Y., Regeneron Genetics Center, Ritchie, M. D., Hyman, M. C., Nazarian, S., Rader, D. J., Voight, B. F. & Damrauer, S. M. Genetics of height and risk of atrial fibrillation: A Mendelian randomization study. PLoS Med. 17, e1003288 (2020).

 

Klarin, D., Verma, S. S., Judy, R., Dikilitas, O., Wolford, B. N., Paranjpe, I., Levin, M. G., Pan, C., Tcheandjieu, C., Spin, J. M., Lynch, J., Assimes, T. L., Nyrønning, L. Å., Mattsson, E., Edwards, T. L., Denny, J., Larson, E., Lee, M. T. M., Carrell, D., Zhang, Y., Jarvik, G. P., Gharavi, A. G., Harley, J., Mentch, F., Pacheco, J. A., Hakonarson, H., Skogholt, A. H., Thomas, L., Gabrielsen, M. E., Hveem, K., Nielsen, J. B., Zhou, W., Fritsche, L., Huang, J., Natarajan, P., Sun, Y. V, DuVall, S. L., Rader, D. J., Cho, K., Chang, K.-M., Wilson, P. W. F., O’Donnell, C. J., Kathiresan, S., Scali, S. T., Berceli, S. A., Willer, C., Jones, G. T., Bown, M. J., Nadkarni, G., Kullo, I. J., Ritchie, M., Damrauer, S. M.* & Tsao, P. S.* Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Circulation CIRCULATIONAHA.120.047544 (2020). doi:10.1161/CIRCULATIONAHA.120.047544

 

Kember, R. L., Merikangas, A. K., Verma, S. S., Verma, A., Judy, R., Regeneron Genetics Center, Damrauer, S. M., Ritchie, M. D., Rader, D. J. & Bućan, M. Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals. Biol. Psychiatry (2020). doi:10.1016/j.biopsych.2020.06.026

 

Vujkovic, M., Keaton, J. M., Lynch, J. A., Miller, D. R., Zhou, J., Tcheandjieu, C., Huffman, J. E., Assimes, T. L., Lorenz, K., Zhu, X., Hilliard, A. T., Judy, R. L., Huang, J., Lee, K. M., Klarin, D., Pyarajan, S., Danesh, J., Melander, O., Rasheed, A., Mallick, N. H., Hameed, S., Qureshi, I. H., Afzal, M. N., Malik, U., Jalal, A., Abbas, S., Sheng, X., Gao, L., Kaestner, K. H., Susztak, K., Sun, Y. V, DuVall, S. L., Cho, K., Lee, J. S., Gaziano, J. M., Phillips, L. S., Meigs, J. B., Reaven, P. D., Wilson, P. W., Edwards, T. L., Rader, D. J., Damrauer, S. M., O’Donnell, C. J., Tsao, P. S., HPAP Consortium, Regeneron Genetics Center, VA Million Veteran Program, Chang, K.-M., Voight, B. F. & Saleheen, D. Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Nat. Genet. (2020). doi:10.1038/s41588-020-0637-y

 

Paranjpe, I., Tsao, N., Judy, R., Paranjpe, M., Chaudhary, K., Klein, D., Forrest, I., O’Hagan, R., Kapoor, A., Pfail, J., Jaladanki, S., Chaudhry, F., Vaid, A., Duy, P. Q., He, J. C., Glicksberg, B. S., Coca, S. G., Gupta, M., Do, R., Damrauer, S. M. & Nadkarni, G. N. Derivation and Validation of Genome Wide Polygenic Score for Urinary Tract Stone Diagnosis. Kidney Int. (2020). doi:10.1016/j.kint.2020.04.055

 

Aragam, K. G., Dobbyn, A., Judy, R., Chaffin, M., Chaudhary, K., Hindy, G., Cagan, A., Finneran, P., Weng, L. C., Loos, R. J. F., Nadkarni, G., Cho, J. H., Kember, R. L., Baras, A., Reid, J., Overton, J., Philippakis, A., Ellinor, P. T., Weiss, S. T., Rader, D. J., Lubitz, S. A., Smoller, J. W., Karlson, E. W., Khera, A. V., Kathiresan, S., Do, R., Damrauer, S. M.* & Natarajan, P.* Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease. J. Am. Coll. Cardiol. 75, 2769–2780 (2020).

 

Kember, R. L., Levin, M. G., Cousminer, D. L., Tsao, N., Judy, R., Schur, G. M., Lubitz, S. A., Ellinor, P. T., McCormack, S. E., Grant, S. F. A., Rader, D. J., Voight, B. F. & Damrauer, S. M. Genetically Determined Birthweight Associates with Atrial Fibrillation: A Mendelian Randomization Study. Circ. Genomic Precis. Med. CIRCGEN.119.002553 (2020). doi:10.1161/CIRCGEN.119.002553

 

Chen, H. Y., Cairns, B. J., Small, A. M., Burr, H. A., Ambikkumar, A., Martinsson, A., Thériault, S., Munter, H. M., Steffen, B., Zhang, R., Levinson, R. T., Shaffer, C. M., Rong, J., Sonestedt, E., Dufresne, L., Ljungberg, J., Näslund, U., Johansson, B., Ranatunga, D. K., Whitmer, R. A., Budoff, M. J., Nguyen, A., Vasan, R. S., Larson, M. G., Harris, W. S., Damrauer, S. M., Stark, K. D., Boekholdt, S. M., Wareham, N. J., Pibarot, P., Arsenault, B. J., Mathieu, P., Gudnason, V., O’Donnell, C. J., Rotter, J. I., Tsai, M. Y., Post, W. S., Clarke, R., Söderberg, S., Bossé, Y., Wells, Q. S., Smith, J. G., Rader, D. J., Lathrop, M., Engert, J. C. & Thanassoulis, G. Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids with Aortic Stenosis. JAMA Cardiol. (2020). doi:10.1001/jamacardio.2020.0246

 

Damrauer, S. M.*, Chaudhary, K.*, Cho, J. H.*, Liang, L. W.*, Argulian, E., Chan, L., Dobbyn, A., Guerraty, M. A., Judy, R., Kay, J., Kember, R. L., Levin, M. G., Saha, A., Van Vleck, T., Verma, S. S., Weaver, J., Abul-Husn, N. S., Baras, A., Chirinos, J. A., Drachman, B., Kenny, E. E., Loos, R. J. F., Narula, J., Overton, J., Reid, J., Ritchie, M., Sirugo, G., Nadkarni*, G., Rader, D. J.* & Do, R*. Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry. JAMA 322: 2191–2202 (2019).

 

Park, J., Levin, M. G., Haggerty, C. M., Hartzel, D. N., Judy, R., Kember, R. L., Reza, N., Ritchie, M. D., Owens, A. T., Damrauer, S. M. & Rader, D. J. A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes. Genet. Med. (2019). doi:10.1038/s41436-019-0625-8

 

Park, J., Damrauer, S. M., Baras, A., Reid, J. G., Overton, J. D. & Gonzalez-Alegre, P. Epidemiology of DYT1 dystonia: Estimating prevalence via genetic ascertainment. Neurol. Genet. 5:e358 (2019).

 

Li, R., Duan, R., Kember, R. L., Rader, D. J., Damrauer, S. M., Moore, J. H. & Chen, Y. A regression framework to uncover pleiotropy in large-scale electronic health record data. J. Am. Med. Inform. Assoc. 26:1083–1090 (2019).

 

Kranzler, H. R., Zhou, H., Kember, R. L., Vickers Smith, R., Justice, A. C., Damrauer, S., Tsao, P. S., Klarin, D., Baras, A., Reid, J., Overton, J., Rader, D. J., Cheng, Z., Tate, J. P., Becker, W. C., Concato, J., Xu, K., Polimanti, R., Zhao, H. & Gelernter, J. Genome-wide association study of alcohol consumption and use disorder in 274,424  individuals from multiple populations. Nat. Commun. 10:1499 (2019).

 

Hoshino, A., Wang, W.-J., Wada, S., McDermott-Roe, C., Evans, C. S., Gosis, B., Morley, M. P., Rathi, K. S., Li, J., Li, K., Yang, S., McMannus, M. J., Bowman, C., Potluri, P., Levin, M., Damrauer, S., Wallace, D. C., Holzbaur, E. L. F. & Arany, Z. The ADP/ATP translocase drives mitophagy independent of nucleotide exchange. Nature (2019). doi:10.1038/s41586-019-1667-4

 

Birtwell, D., Williams, H., Pyeritz, R., Damrauer, S. & Mowery, D. L. Carnival: A Graph-Based Data Integration and Query Tool to Support Patient Cohort Generation for Clinical Research. Stud. Health Technol. Inform. 264:35–39 (2019).

 

AlDubayan, S. H., Pyle, L. C., Gamulin, M., Kulis, T., Moore, N. D., Taylor-Weiner, A., Hamid, A. A., Reardon, B., Wubbenhorst, B., Godse, R., Vaughn, D. J., Jacobs, L. A., Meien, S., Grgic, M., Kastelan, Z., Markt, S. C., Damrauer, S. M., Rader, D. J., Kember, R. L., Loud, J. T., Kanetsky, P. A., Greene, M. H., Sweeney, C. J., Kubisch, C., Nathanson, K. L., Van Allen, E. M., Stewart, D. R. & Lessel, D. Association of Inherited Pathogenic Variants in Checkpoint Kinase 2 (CHEK2) With  Susceptibility to Testicular Germ Cell Tumors. JAMA Oncol. 5:514–522 (2019).

 

Small, A. M., Kiss, D. H., Anwaruddin, S., Giri, J., Han, Y., Zhao, L., Salvador, L., Cvijic, M. E., Li, Z., Chirinos, J. A., Damrauer, S. M. & Rader, D. J. Soluble FMS-Like Tyrosine Kinase-1 Is a Circulating Biomarker Associated With Calcific Aortic Stenosis. J. Am. Coll. Cardiol. 73:1364–1365 (2019).

 

Haggerty, C. M.*, Damrauer, S. M.*, Levin, M. G., Birtwell, D., Carey, D. J., Golden, A. M., Hartzel, D. N., Hu, Y., Judy, R., Kelly, M. A., Kember, R. L., Kirchner, H. L., Leader, J. B., Liang, L., McDermott-Roe, C., Babu, A., Morley, M., Nealy, Z., Person, T. N., Pulenthiran, A., Small, A., Smelser, D. T., Stahl, R. C., Sturm, A. C., Williams, H., Baras, A., Margulies, K. B., Cappola, T. P., Dewey, F. E., Verma, A., Zhang, X., Correa, A., Hall, M. E., Wilson, J. G., Ritchie, M. D., Rader, D. J., Murray, M. F., Fornwalt, B. K., Arany, Z. & DiscovEHR and Penn Medicine Biobank Studies. Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants. Circulation 140:42-54 (2019).

 

Damrauer, S. M.*, Hardie, K.*, Kember, R. L., Judy, R., Birtwell, D., Williams, H., Rader, D. J. & Pyeritz, R. E. FBN1 Coding Variants and Nonsyndromic Aortic Disease. Circ. Genomic Precis. Med. 12:e002454 (2019).

 

Levin, M. G., Kember, R. L., Judy, R., Birtwell, D., Williams, H., Arany, Z., Giri, J., Guerraty, M., Cappola, T. P., Regeneron Genetics Center, Chen, J., Rader, D. J. & Damrauer, S. M. Genomic Risk Stratification Predicts All-Cause Mortality After Cardiac Catheterization. Circ. Genomic Precis. Med. 1–7 (2018).

 

Klarin, D.*, Damrauer, S. M.*, Cho, K., Sun, Y. V, Teslovich, T. M., Honerlaw, J., Gagnon, D. R., DuVall, S. L., Li, J., Peloso, G. M., Chaffin, M., Small, A. M., Huang, J., Tang, H., Lynch, J. A., Ho, Y.-L., Liu, D. J., Emdin, C. A., Li, A. H., Huffman, J. E., Lee, J. S., Natarajan, P., Chowdhury, R., Saleheen, D., Vujkovic, M., Baras, A., Pyarajan, S., Angelantonio, E., Neale, B. M., Naheed, A., Khera, A. V, Danesh, J., Chang, K.-M., Abecasis, alo, Willer, C., Dewey, F. E., Carey, D. J., Concato, J., Michael Gaziano, J., Oamp, C. J., Tsao, P. S., Kathiresan, S., Rader, D. J., F Wilson, P. W. & Assimes, T. L. Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. Nat. Genet. (2018).

 

Roselli, C., Chaffin, M. D., Weng, L.-C., Aeschbacher, S., Ahlberg, G., Albert, C. M., Almgren, P., Alonso, A., Anderson, C. D., Aragam, K. G., Arking, D. E., Barnard, J., Bartz, T. M., Benjamin, E. J., Bihlmeyer, N. A., Bis, J. C., Bloom, H. L., Boerwinkle, E., Bottinger, E. B., Brody, J. A., Calkins, H., Campbell, A., Cappola, T. P., Carlquist, J., Chasman, D. I., Chen, L. Y., Chen, Y.-D. I., Choi, E.-K., Choi, S. H., Christophersen, I. E., Chung, M. K., Cole, J. W., Conen, D., Cook, J., Crijns, H. J., Cutler, M. J., Damrauer, S. M., Daniels, B. R., Darbar, D., Delgado, G., Denny, J. C., Dichgans, M., Dörr, M., Dudink, E. A., Dudley, S. C., Esa, N., Esko, T., Eskola, M., Fatkin, D., Felix, S. B., Ford, I., Franco, O. H., Geelhoed, B., Grewal, R. P., Gudnason, V., Guo, X., Gupta, N., Gustafsson, S., Gutmann, R., Hamsten, A., Harris, T. B., Hayward, C., Heckbert, S. R., Hernesniemi, J., Hocking, L. J., Hofman, A., Horimoto, A. R. V. R., Huang, J., Huang, P. L., Huffman, J., Ingelsson, E., Ipek, E. G., Ito, K., Jimenez-Conde, J., Johnson, R., Jukema, J. W., Kääb, S., Kähönen, M., Kamatani, Y., Kane, J. P., Kastrati, A., Kathiresan, S., Katschnig-Winter, P., Kavousi, M., Kessler, T., Kietselaer, B. L., Kirchhof, P., Kleber, M. E., Knight, S., Krieger, J. E., Kubo, M., Launer, L. J., Laurikka, J., Lehtimäki, T., Leineweber, K., Lemaitre, R. N., Li, M., Lim, H. E., Lin, H. J. H., Lin, H. J. H., Lind, L., Lindgren, C. M., Lokki, M.-L., London, B., Loos, R. J. F., Low, S.-K., Lu, Y., Lyytikäinen, L.-P., Macfarlane, P. W., Magnusson, P. K., Mahajan, A., Malik, R., Mansur, A. J., Marcus, G. M., Margolin, L., Margulies, K. B., März, W., McManus, D. D., Melander, O., Mohanty, S., Montgomery, J. A., Morley, M. P., Morris, A. P., Müller-Nurasyid, M., Natale, A., Nazarian, S., Neumann, B., Newton-Cheh, C., Niemeijer, M. N., Nikus, K., Nilsson, P., Noordam, R., Oellers, H., Olesen, M. S., Orho-Melander, M., Padmanabhan, S., Pak, H.-N., Paré, G., Pedersen, N. L., Pera, J., Pereira, A., Porteous, D., Psaty, B. M., Pulit, S. L., Pullinger, C. R., Rader, D. J., Refsgaard, L., Ribasés, M., Ridker, P. M., Rienstra, M., Risch, L., Roden, D. M., Rosand, J., Rosenberg, M. A., Rost, N., Rotter, J. I., Saba, S., Sandhu, R. K., Schnabel, R. B., Schramm, K., Schunkert, H., Schurman, C., Scott, S. A., Seppälä, I., Shaffer, C., Shah, S., Shalaby, A. A., Shim, J., Shoemaker, M. B., Siland, J. E., Sinisalo, J., Sinner, M. F., Slowik, A., Smith, A. V., Smith, B. H., Smith, J. G. D., Smith, J. G. D., Smith, N. L., Soliman, E. Z., Sotoodehnia, N., Stricker, B. H., Sun, A., Sun, H., Svendsen, J. H., Tanaka, T., Tanriverdi, K., Taylor, K. D., Teder-Laving, M., Teumer, A., Thériault, S., Trompet, S., Tucker, N. R., Tveit, A., Uitterlinden, A. G., Van Der Harst, P., Van Gelder, I. C., Van Wagoner, D. R., Verweij, N., Vlachopoulou, E., Völker, U., Wang, B., Weeke, P. E., Weijs, B., Weiss, R., Weiss, S., Wells, Q. S., Wiggins, K. L., Wong, J. A., Woo, D., Worrall, B. B., Yang, P.-S., Yao, J., Yoneda, Z. T., Zeller, T., Zeng, L., Lubitz, S. A., Lunetta, K. L. & Ellinor, P. T. Multi-ethnic genome-wide association study for atrial fibrillation. Nat. Genet. 50: 1225–1233 (2018).

 

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